Prenatal exposure to environmentally relevant levels of PBDE-99 leads to testicular dysgenesis with steroidogenesis disorders

Polybrominated diphenyl ethers (PBDEs) are a widely used class of brominated flame retardants. Exposure to PBDEs could induce testicular damage in mammals, but the effects and potential mechanism of action of prenatal exposure to environmentally relevant PBDEs on testicular development remain unclea...

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Veröffentlicht in:Journal of hazardous materials 2022-02, Vol.424 (Pt B), p.127547, Article 127547
Hauptverfasser: Zhao, Tianxin, Tang, Xiangliang, Li, Dian, Zhao, Jinglu, Zhou, Rui, Shu, Fangpeng, Jia, Wei, Fu, Wen, Xia, Huimin, Liu, Guochang
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Sprache:eng
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Zusammenfassung:Polybrominated diphenyl ethers (PBDEs) are a widely used class of brominated flame retardants. Exposure to PBDEs could induce testicular damage in mammals, but the effects and potential mechanism of action of prenatal exposure to environmentally relevant PBDEs on testicular development remain unclear. For the in vivo study, pregnant ICR mice were exposed to environmentally relevant levels of 2,2′,4,4′,5-pentabromodiphenyl ether (PBDE-99), a major component of commercial PBDE mixtures. We found that the anogenital index and testicular organ coefficient were significantly decreased, the incidence of cryptorchidism was increased, and testicular histology was disturbed in male offspring. Transcriptomic profiling showed that steroidogenesis disorders were significant in all PBDE-99 exposure groups. The testosterone levels, expressions of testosterone regulators, and the number of CYP11A1-positive and 11β-HSD1-positive Leydig cells were significantly decreased after PBDE-99 exposure. For the in vitro study, TM3 Leydig cells were exposed to PBDE-99 at gradient concentrations. Transcriptomic profiling and validation experiments showed that PBDE-99 upregulated reactive oxygen species, activated the ERK1/2 pathway, inhibited the ubiquitination degradation pathway, and finally induced Leydig cell apoptosis. Cumulatively, these findings revealed that prenatal exposure to environmentally relevant levels of PBDE-99 leads to steroidogenesis disorders by inducing the apoptosis of Leydig cells, causing testicular dysgenesis. [Display omitted] •Prenatal exposure to environment related PBDE-99 leads to testicular dysgenesis.•Steroidogenesis disorder is involved in PBDE-99-induced testicular dysgenesis.•PBDE-99 exposure promotes cell apoptosis in immature Leydig cells.•PBDE-99 increases ROS levels and activates the ERK1/2 pathway in Leydig cells.•PBDE-99 inhibits the ubiquitination degradation pathway in Leydig cells.
ISSN:0304-3894
1873-3336
DOI:10.1016/j.jhazmat.2021.127547